At a Glance
- Tasks: Lead the EU Regulatory Services team and drive sales for innovative regulatory solutions.
- Company: Global leader in providing essential information for healthcare and scientific research.
- Benefits: Competitive salary, career development opportunities, and a dynamic work environment.
- Other info: Join a collaborative culture focused on innovation and excellence.
- Why this job: Make a real impact in the life sciences industry while leading a talented team.
- Qualifications: Bachelor’s degree in life sciences or tech, with significant pharmaceutical experience.
The predicted salary is between 60000 - 60000 £ per year.
- Location & Salary
- Central London / West End
- Company Overview
Our Client is a global leader in providing essential information to the world's businesses and professionals, Healthcare and Scientific Research.
The Scientific business of Our Client provides information and knowledge to accelerate research, discovery and innovation.
Their authoritative, accurate and timely information is essential for drug companies to discover new drugs and get them to market faster; researchers to find relevant papers and know what’s newly published in their subject; and businesses to optimize their intellectual property and find competitive intelligence.
Mention of Liquent
Our Client has a product called Liquent, which is the global leader in providing regulatory software solutions, information products and related services for the life sciences industry.
Liquent’s software and service offerings help to ensure that clients meet the strict standard of regulatory authorities across the world, helping them achieve quality, accuracy and data integrity to deliver regulatory reports and submissions reliably and on time.
Position Summary
Due to continued success Our Client has a new, exciting and challenging opportunity for a Director, EU Regulatory Services.
The Director, EU Regulatory Services will be expected to direct the EU Regulatory Services team and drive Liquent Direct Outsourcing sales in Europe working closely with the Sales Director, Europe to achieve targeted goals.
Liquent Direct services include submission outsourcing, project management, e-CTD preparedness and education, submission publishing and submission publishing strategy.
Responsibilities include revenue forecasting, EU sales support, customer presentations, management of European Regulatory Services revenue and career development for the EU Regulatory Services Team.
Qualifications
- Bachelor’s degree or equivalent in life sciences or technology-related discipline.
- Significant pharmaceutical industry experience. End-to-end regulatory submission publishing and document management experience required with demonstrable management experience.
- Leadership, project management, and public speaking experience required.
- An understanding of global regulatory submission formats, industry standards, and guidelines, software validation concepts, and publishing best practices.
- An understanding of the Life Sciences Business, specifically in the pharmaceutical environment pertaining to regulatory guidance and regulatory submission assembly.
- Proficiency working in Microsoft Windows environment and with Windows-based applications including, but not limited to, Microsoft Office products, Adobe Acrobat, desktop publishing and graphics packages.
- Experience with publishing software In Sight Publisher, Core Dossier and EZsub as well as other Liquent products considered a plus.
- Strong organizational and interpersonal skills, this individual should be detail oriented with a strong customer service focus.
- Strong written and oral communication skills, including public speaking in formal and informal educational environments.
- The ability to work well independently and in a team environment.
- Ability to build strong relationships with global regulatory authorities.
- Management and supervisory experience.
- Familiarity with the audit process.
To apply for this job or for info on our other jobs email
#J-18808-Ljbffr
